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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name tube, feeding
510(k) Number K890116
Device Name ENTERAL FEEDING TUBE
Applicant
HDC CORP.
2551 CASEY AVE.
MOUNTAIN VIEW,  CA  94043
Applicant Contact L COLEMAN
Correspondent
HDC CORP.
2551 CASEY AVE.
MOUNTAIN VIEW,  CA  94043
Correspondent Contact L COLEMAN
Regulation Number876.5980
Classification Product Code
FPD  
Date Received01/11/1989
Decision Date 04/05/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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